Barbry P, Simon-Bouy B, Mattéi M G, Le Guern E, Jaume-Roig B, Chassande O, Ullrich A, Lazdunski M
Institut de Pharmacologie Moléculaire et Cellulaire, UPR 411 CNRS, Valbonne, France.
Hum Genet. 1990 Oct;85(6):587-9. doi: 10.1007/BF00193579.
The apical sodium channel is essential for sodium reabsorption by the kidney. Its activity is blocked by the diuretic amiloride. Using a human cDNA coding for the amiloride binding protein (ABP), the corresponding structural gene was mapped to human chromosome 7q34-q36 by in situ hybridization. This region flanks the region implicated in cystic fibrosis (7q32). Because an alteration of the amiloride sensitive sodium channel function has been suggested in cystic fibrosis, a possible link between the ABP gene and this disease was analyzed by restriction fragments length polymorphism (RFLP) analyses. From this study, it appears that the gene coding for ABP is not directly modified by mutations causing cystic fibrosis.
顶端钠通道对肾脏重吸收钠至关重要。其活性被利尿药氨氯吡脒阻断。利用编码氨氯吡脒结合蛋白(ABP)的人cDNA,通过原位杂交将相应的结构基因定位于人染色体7q34 - q36。该区域毗邻与囊性纤维化相关的区域(7q32)。由于有人提出囊性纤维化中氨氯吡脒敏感钠通道功能存在改变,因此通过限制性片段长度多态性(RFLP)分析来研究ABP基因与该疾病之间可能的联系。从这项研究来看,编码ABP的基因似乎不会因导致囊性纤维化的突变而直接发生改变。